Variant report

Variant	rs12265141
Chromosome Location	chr10:23326796-23326797
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:23324600-23328000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr10:23325400-23326800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr10:23326200-23326800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr10:23326200-23326800	Active TSS	Brain Cingulate Gyrus	brain
5	chr10:23326200-23327000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr10:23326400-23326800	Active TSS	Brain Hippocampus Middle	brain
7	chr10:23326400-23326800	Enhancers	Brain Inferior Temporal Lobe	brain
8	chr10:23326400-23326800	Enhancers	Fetal Lung	lung
9	chr10:23326400-23327400	Weak transcription	Brain Substantia Nigra	brain
10	chr10:23326400-23327800	Weak transcription	Brain Angular Gyrus	brain
11	chr10:23326600-23326800	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr10:23326600-23326800	Enhancers	K562	blood

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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